|Publication number||US7361146 B1|
|Application number||US 11/416,317|
|Publication date||Apr 22, 2008|
|Filing date||May 1, 2006|
|Priority date||Nov 24, 2004|
|Publication number||11416317, 416317, US 7361146 B1, US 7361146B1, US-B1-7361146, US7361146 B1, US7361146B1|
|Inventors||Rupinder Bharmi, Gene A. Bornzin|
|Original Assignee||Pacesetter, Inc.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (34), Non-Patent Citations (16), Referenced by (26), Classifications (37), Legal Events (3)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a continuation-in-part of U.S. patent application Ser. No. 11/127,389, filed May 11, 2005, entitled “System and Method for Detection of Respiration Patterns via Intracardiac Electrogram Signals”, which claimed the benefit of U.S. Provisional Patent Application Ser. No. 60/631,111, filed Nov. 24, 2004.
The invention generally relates to implantable medical devices, such as pacemakers or implantable cardioverter/defibrillators (ICDs), and in particular, to techniques for detecting respiration patterns within a patient in which a medical device is implanted, including abnormal respiration patterns such as apnea, hypopnea or nocturnal asthma.
It is highly desirable to reliably track respiration within patients having pacemakers and ICDs. Tracking patient respiration permits potentially dangerous respiratory disorders, such as apnea, hypopnea, hyperpnea, nocturnal asthma, and Cheyne-Stokes Respiration (CSR), to be detected. Apnea and hypopnea are abnormal respiration patterns characterized by periods of significantly reduced respiration. With hypopnea, respiration is reduced but still present. With apnea, however, respiration may cease completely for 10 seconds or longer. One common form of apnea is sleep apnea, in which hundreds of individual episodes of apnea can occur during a single night. Accordingly, patients with sleep apnea experience frequent wakefulness at night and excessive sleepiness during the day. In addition, apnea can exacerbate various medical conditions, particularly congestive heart failure (CHF) wherein the patient suffers from poor cardiac function. Indeed, the aberrant blood chemistry levels occurring during sleep apnea are a significant problem for patients with CHF. Due to poor cardiac function caused by CHF, patients already suffer from generally low blood oxygen levels. Frequent periods of sleep apnea result in even lower blood oxygen levels.
Episodes of apnea can also occur during CSR, which is an abnormal respiratory pattern often occurring in patients with CHF. CSR is characterized by alternating periods of hypopnea and hyperpnea (i.e. fast, deep breathing.) Briefly, CSR arises principally due to a time lag between blood CO2 levels sensed by the respiratory control nerve centers of the brain and the blood CO2 levels. With CHF, poor cardiac function results in poor blood flow to the brain such that respiratory control nerve centers respond to blood CO2 levels that are no longer properly representative of the overall blood CO2 levels in the body. Hence, the respiratory control nerve centers trigger an increase in the depth and frequency of breathing in an attempt to compensate for perceived high blood CO2 levels—although the blood CO2 levels have already dropped. By the time the respiratory control nerve centers detect the drop in blood CO2 levels and act to slow respiration, the blood CO2 levels have already increased. This cycle becomes increasingly unbalanced until respiration alternates between hypopnea and hyperpnea. The periods of hypopnea often become sufficiently severe that no breathing occurs between the periods of hyperpnea, i.e. periods of frank apnea occur between the periods of hyperpnea. The wildly fluctuating blood chemistry levels caused by alternating between hyperpnea and apnea/hypopnea can significantly exacerbate CHF and other medical conditions. When CHF is still mild, CSR usually occurs, if at all, only while the patient is sleeping. When it becomes more severe, CSR can occur while the patient is awake.
Abnormal respiration during sleep may also arise due to nocturnal asthma. With asthma, the linings of the airways swell and become more inflamed. Mucus clogs the airways and the muscles around the airways tighten and narrow. Hence, breathing becomes difficult and stressful. During an asthma attack, rapid breathing patterns similar to hyperpnea occur, though little or no oxygen actual reaches the lungs. An asthma attack may be triggered by allergens, respiratory infections, cold and dry air, or even heartburn. The majority of asthma attacks occur during the night, between 3:00 a.m. and 5:00 a.m. Nocturnal asthma has been associated with factors such as decreased pulmonary function, hypoxemia and circadian variations of histamine, epinephrine, and cortisol concentrations. Asthma attacks at night may also be triggered directly by sleep apnea. Nocturnal asthma attacks may be fatal, particularly within patients also suffering from CHF.
In view of the significant adverse consequences of apnea/hypopnea, nocturnal asthma, or CSR, particularly insofar as patients with CHF are concerned, it is highly desirable to provide techniques for detecting such conditions. Tracking actual patient respiration provides perhaps the most direct and effective technique for detecting respiratory disorders. For patients with pacemakers and ICDs, respiration is conventionally tracked based on thoracic impedance as measured via pacing/sensing leads implanted within the heart. Sensing of the intracardiac electrogram (IEGM) of the patient is temporarily suspended during each cardiac cycle so as to sense an impedance signal, from which respiration patterns are derived. See, for example, U.S. Pat. No. 6,449,509 to Park, et al., entitled “Implantable Stimulation Device Having Synchronous Sampling for a Respiration Sensor.”
Although impedance-based techniques are useful, it would be desirable to provide alternative techniques for tracking respiration, particularly for the purposes of detecting episodes of abnormal respiration, wherein respiration is derived solely from the IEGM signal so as to eliminate the need to detect or process impedance. Additionally, this eliminates need for additional sensors, and the sensing electrodes can be thus used for IEGM based breathing pattern detection and hence, the ease of implementability in current platforms. One technique for deriving respiration from an IEGM signal is set forth in U.S. Pat. No. 6,697,672 to Andersson, entitled “Implantable Heart Stimulator”, which is incorporated by reference herein. Briefly, Andersson provides a technique to extract parameters related to patient respiration from an analysis of intervals between various events detected within a ventricular-IEGM (i.e. V-IEGM) signal. For example, cycle-to-cycle variability is tracked in R-R intervals or in the amplitude of S-T intervals. In other words, the technique of Andersson exploits interval-based morphological features of the V-IEGM to track respiration. Although not discussed in the Andersson reference, autonomic variability arising during respiration causes the interval-based changes in the IEGM. R-waves (also referred to as QRS-complexes) are electrical signals representative of the depolarization of ventricular muscle tissue. The subsequent electrical repolarization of the ventricular tissue appears within the IEGM as a T-wave. Electrical depolarization of atrial muscle tissue is manifest as a P-wave. Strictly speaking, P-waves, R-waves and T-waves are features of a surface electrocardiogram (EKG or ECG). For convenience, the terms P-wave, R-wave and T-wave are also used herein (and in the literature) to refer to the corresponding internal signal component.
Although the interval-based variability technique of Andersson is effective, it is desirable to provide additional or alternative IEGM-based techniques for trending and tracking respiration and for detecting episodes of abnormal respiration. This general goal was achieved by the techniques of the parent application, cited above. Briefly, respiration patterns are detected based upon cycle-to-cycle changes in morphological features associated with individual electrical events with the IEGM signals. For example, slight changes in the peak amplitudes of QRS-complexes, P-waves or T-waves are tracked to identify cyclical variations representative of patient respiration. Alternatively, the integrals of the morphological features of the individual events may be calculated for use in tracking respiration. Once respiration patterns have been identified, episodes of abnormal respiration, such as apnea, hyperpnea, nocturnal asthma, or the like, may be detected and therapy automatically delivered.
Hence, the techniques of the parent application, which are also described herein below, are not limited to analyzing interval-based features of a V-IEGM, as with certain predecessor techniques. Instead, the techniques of the parent application examine changes within individual features of cardiac cycles over time. In this regard, it has been observed that respiration causes slight variations in the size and shape of individual electrical events of the IEGM signals, such as QRS-complexes, and that those changes are correlated with respiration. This differs from changes in intervals (such as R-R intervals), which, as noted, appear to arise due to autonomic variability. In one specific example, changes in the integrals of the QRS-complex derived from a V-IEGM channel signal are examined, alone or in combination with, integrals of P-waves derived from an atrial IEGM (A-IEGM) channel signal. Interval-based parameters, such as variations in A-A, R-R or AV intervals, may be additionally used to aid in tracking respiration but are not required.
The parent application also presented techniques for detecting episodes of abnormal respiration based on respiration patterns, such as episodes of such as apnea, hypopnea, nocturnal asthma, or CSR. The present application is primarily directed to providing further improvements in the area of abnormal respiration detection.
In accordance with one illustrative embodiment, techniques are provided for detecting abnormal respiration within a patient using an implantable medical device. In one example, IEGM signals are sensed and individual cardiac cycles are identified therein. Selected individual electrical events (such as P-waves, QRS-complexes or T-waves) are identified within the cardiac cycles and one or more morphological or temporal parameters associated with the individual features are detected (such as maximum amplitude, peak-to-peak amplitude, or numerical integral of the feature). Patient respiration is detected based on cycle-to-cycle changes in the detected parameters associated with the individual selected electrical events. Then, abnormal respiration is detected by identifying individual respiratory cycles within the patient respiration, detecting one or more parameters associated with the individual respiratory cycles, detecting any significant changes in the parameters associated with the individual respiratory cycles, and then evaluating the significant changes to detect abnormal respiration. Exemplary parameters associated with the individual respiratory cycles include the inter-breath interval, respiration depth, standard deviation in respiration depth, and median respiration depth. Respiration power, which may encompass multiple respiratory cycles, is also preferably determined.
Hence, in the example, episodes of abnormal respiration—such as apnea, hypopnea, nocturnal asthma, or CSR—are detected based on significant changes in respiratory parameters, which are in turn derived from the morphological and temporal parameters of cardiac cycles within the IEGM. The techniques are particularly well suited to detecting episodes of abnormal respiration during sleep. In this regard, normal respiration during sleep is characterized by an almost constant respiration depth (corrected for patient posture and other non-respiratory factors). Hence, significant changes in respiration depth or other parameters associated with the respiratory cycles are indicative of a transition from normal respiration to some form of abnormal respiration. Further analysis of the respiratory parameters is used to identify the particular form of abnormal respiration. The technique can also be used to track and trend sleep disorder breathing or, in general, disordered breathing. Depending upon the capabilities of the implanted device, appropriate therapy may then be delivered. For example, an alarm device may be triggered to alert the patient upon detection of an episode of apnea/hypopnea. The alarm device may be, e.g., an implanted device such as a “tickle” voltage warning device or a bedside warning system that emits an audible alarm. In this manner, if the patient is asleep, the patient is thereby awakened so as to prevent extended episodes of apnea/hypopnea from occurring, which can cause significant variances in blood chemistry that can exacerbate other medical conditions such as CHF.
In addition, if a determination has been made by the implanted system that the patient is subject to frequent episodes of apnea or hypopnea, dynamic atrial overdrive (DAO) pacing may be delivered in an effort to prevent additional episodes from occurring. If an implantable drug pump is provided, the implanted system may be programmed to selectively deliver medications deemed effective in addressing abnormal respiration or effective in addressing the underlying medical condition causing the abnormal respiration (which may be, e.g., CHF). In addition, regardless of the type of therapy, diagnostic information is preferably recorded within a memory of the implanted system for subsequent review by a physician.
Thus, by analyzing respiratory parameters derived from IEGM signals, abnormal respiration can be detected using a pacemaker or ICD without requiring additional leads or sensors beyond those otherwise employed in cardiac sensing/pacing. In the alternative, the detection techniques of the invention may be implemented within other implantable devices besides pacemakers or ICDs, such as dedicated devices provided specifically for detecting episodes of abnormal respiration.
The above and further features, advantages and benefits of the invention will be apparent upon consideration of the descriptions herein taken in conjunction with the accompanying drawings, in which:
The following description includes the best mode presently contemplated for practicing the invention. This description is not to be taken in a limiting sense but is made merely to describe general principles of the invention. The scope of the invention should be ascertained with reference to the issued claims. In the description of the invention that follows, like numerals or reference designators are used to refer to like parts or elements throughout.
Overview of Implantable Medical System
Once an episode of abnormal respiration has been detected, the pacer/ICD uses additional implanted components (if so equipped) to deliver appropriate therapy or warning signals. For example, if apnea/hypopnea is detected, the pacer/ICD may activate an internal alarm 18 or an external bedside alarm 22. Internal alarm 18 may be a vibrating device or a “tickle” voltage device that, in either case, provides perceptible stimulation to the patient to alert or awaken the patient so as to terminate the episode of apnea/hypopnea. The bedside alarm may provide audible or visual alarm signals of sufficient magnitude to alert or awaken the patient. If an activity sensor is provided within the pacer/ICD, the form of the alarm may be controlled based on patient activity. For example, if the activity level indicates that the patient is asleep, a more noticeable alarm may be employed than if the patient is deemed to be awake. In addition, while the patient is asleep, the intensity of the alarm signal can be periodically increased until the patient awakens, as detected by the activity sensor. Additionally, or in the alternative, the system may include a drug pump 20 capable of the delivering medications in an attempt to prevent the onset of additional episodes of apnea/hypopnea. Discussions of exemplary medications are provided below. In addition, the pacer/ICD may deliver atrial overdrive pacing for the purposes of preventing additional episodes of apnea/hypopnea from occurring.
Overview of Technique for Tracking Respiration Using IEGM
Then, at step 108, patient respiration is detected based on cycle-to-cycle changes in the morphological parameters (such as cycle-to-cycle variations in the integral of the QRS-complexes or cycle-to-cycle changes in the maximum amplitudes of P-waves). In other words, changes in morphology of a given parameter from one beat to another are tracked for the purposes of detecting respiration patterns. This differs from changes in intervals (such as R-R intervals), which, as noted above, appear to arise due to autonomic variability.
The slight variations in the morphology of individual events within the IEGM are tracked from cycle-to-cycle so as to detect the cyclical changes associated with normal respiration. Otherwise conventional filters may be used to isolate cyclical patterns appearing at frequencies associated with respiration. Additionally, an analysis of changes in the intervals between beats may be used to enhance the reliability of the respiration detection technique of step 108. In particular, the techniques described in the above-referenced patent to Andersson may be employed. Variability in AV or A-A intervals may also be employed. In other words, both interval-based and individual feature-based techniques may be employed to enhance detection specificity.
Depolarization-Based Respiration Detection Examples
Turning now to the
Specific examples are illustrated in
The integrals from the VERs of graph 212 have been connected by an interpolated line so as to provide a smooth representation of the respiration pattern of the canine test subject. More complex methods may be used to interpolate by using curve fitting of functions or by using a reconstruction filter. When a patient is awake/active, curve fitting can instead be used to provide smooth representation to calculate the breathing rate. As can be seen, there is clearly a cyclical pattern composed of alternating peaks and nadirs, from which respiration information may be derived. In particular, the rate of respiration may be derived (using otherwise conventional signal processing and analysis techniques) based upon the interval from one peak to another or the interval from one nadir to another. The relative amplitude of respiration may be derived based on comparison of the amplitude of the respective peaks and nadir of a given respiration cycle. Hence, although the respiration pattern of graph 214 does not necessarily closely represent an actual canine respiration pattern (which is typically more sinusoidal, particularly during fairly fast-paced respiration), the respiration pattern of graph 214 is nevertheless sufficient to obtain gross information pertaining to respiration, such as rate and relative amplitude from which episodes of abnormal respiration may be detected.
A second depolarization-based example is shown in
Another depolarization-based example is shown in
Repolarization-Based Respiration Detection Examples
Turning now to the
Specific T-wave-based examples are illustrated in
A second repolarization-based example is shown in
Another repolarization-based example is shown in
Interval-Based Respiration Detection Examples
In addition to the aforementioned beat-by-beat tracking techniques, which seek to track respiration based on changes in morphology, intervals between successive beats (or between successive features of an individual beat) may additionally, or alternatively, be employed. This is summarized in
The use of changes in R-R and ST intervals derived from V-IEGM signals are described in detail with reference to the Andersson cited above. The technique of
Abnormal Respiration Detection and Therapy
What have been described thus far are various techniques for tracking respiration patterns based on features of IEGM signals. With reference to
Briefly, apnea may be detected based upon a lack of any significant amplitude variations within the detected respiration patterns extending over a predetermined period of time. In one example, an apnea detection amplitude threshold value may be specified along with an apnea detection time threshold value. If the respiratory amplitude derived from the respiration patterns does not exceed the amplitude threshold value for at least a period of time greater than the time threshold value, then apnea is presumed. Typically, an episode of apnea is not deemed to have occurred unless there is a lack respiration for at least ten seconds and so a time threshold of at least ten seconds may be employed. A suitable amplitude threshold value may be determined via routine experimentation for use with respiration patterns derived from particular IEGM parameters. In this regard, the amplitude threshold value for use with the respiration patterns derived from QRS-complexes may differ from one derived from the P-waves or T-waves. The values may also differ from patient to patient. Note that the amplitude and morphology changes may also depend on body position, and also on the rhythm types, i.e. in case of a pacer/ICD, it would be advisable to have different thresholds for different rhythm combinations: A-R, A-V, P-R, P-V. Suitable amplitude threshold values may be specified following implant of device based on the specific characteristics of patient in which the device is implanted or automatically updated during routine working of the algorithm.
More complex techniques may be employed identifying each episode of apnea. In one example, a combination of raw respiration parameters generated above and various thresholds on each parameter are fed into an apnea episode detection system, specifically configured for detecting apnea. Additionally, simple or more complex methods than zero crossings can be used to determine breathing rate. Depth of breathing and effort of breathing can be calculated. The local variability in each parameter as derived from mean and stand-deviations etc. may also be fed as variables into the apnea episode detection system. (Other variables that can be derived include median, peak-to-peak changes, and inter-quartile range.) Using the long term autonomic interval-based variability as well as the individual event-based morphological variability, it is possible to detect differences between obstructive apnea, central apnea, nocturnal apnea, CSA and flow hypopnea etc.
Hypopnea may be detected based upon respiratory amplitude that exceeds the apnea threshold but falls below a separate hypopnea amplitude threshold. As with apnea, a time threshold value (such as 10 seconds) may be specified as well. Hence, if there is at least some respiration, but the amplitude of that respiration falls below an amount deemed healthy for the patient, hypopnea is presumed. As with the various apnea thresholds, separate hypopnea threshold values may be specified for use with different respiration detection techniques (i.e. depolarization-based techniques versus repolarization-based techniques) and for use with different patients, preferably determined on a patient by patient basis following implant of the device. Alternative and more complex hypopnea detection techniques may be employed as well.
Hyperpnea/asthma may be detected based upon a pattern exhibiting excessively rapid respiration (or attempted respiration.) Accordingly, an hyperpnea/asthma amplitude detection threshold may be specified along with a hyperpnea/asthma respiration rate and effort threshold. If amplitude derived from the respiration pattern exceeds the hyperpnea/asthma respiration amplitude detection threshold while the respiration rate (also derived from the respiration pattern) also exceeds it respective threshold, hyperpnea/asthma is thereby presumed. Again, suitable thresholds may be determined on the patient basis following implant of device. Alternative and more complex hyperpnea/asthma or CSR detection techniques may be employed as well.
Hyperpnea usually may be distinguished from asthma based on the presence or absence of normal respiration preceding the attack. Hyperpnea usually follows an episode of apnea/hypopnea; whereas asthma usually follows a period of otherwise normal breathing. Episodes of nocturnal asthma may be distinguished from other asthma attacks merely by determining whether the patient is asleep, using otherwise conventional sleep detection techniques. Examples of sleep detection techniques are set forth in: U.S. Pat. No. 5,476,483, to Bornzin et al., entitled “System and Method for Modulating the Base Rate During Sleep for a Rate-responsive Cardiac Pacemaker” and U.S. Pat. No. 6,128,534 to Park et al., entitled “Implantable Cardiac Stimulation Device And Method For Varying Pacing Parameters To Mimic Circadian Cycles.”
CSR may be detected using otherwise conventional techniques based on its characteristic pattern of alternating periods of apnea/hypopnea and hyperpnea. See, e.g., U.S. Pat. No. 6,830,548 to Bonnet, et al., “Active Medical Device Able to Diagnose a Patient Respiratory Profile.”
Once an episode of abnormal respiration has been detected then, at step 452, the pacer/ICD delivers appropriate therapy (assuming it is properly equipped). For example, in response to detection of frequent episodes of apnea/hypopnea, atrial overdrive pacing therapy may be applied in an attempt to prevent the onset of additional episodes. A particularly effective atrial overdrive pacing technique, referred to herein as dynamic atrial overdrive (DAO) pacing, is described in U.S. Pat. No. 6,519,493 to Florio et al., entitled “Methods and Apparatus for Overdrive Pacing Heart Tissue Using an Implantable Cardiac Stimulation Device”. Routine experimentation may be performed to identify optimal DAO pacing parameters for use with patients with apnea/hypopnea. The aggressiveness of DAO therapy may be adjusted based upon the frequency or duration of episodes of apnea/hypopnea.
Anti-apneic medications may be delivered via an implantable drug pump, if so equipped. Examples of medications that may be helpful in patients with apnea are set forth the following U.S. Pat. Nos. 6,331,536 to Radulovacki, et al., entitled “Pharmacological Treatment for Sleep Apnea”; 6,432,956 to Dement, et al., entitled “Method for Treatment of Sleep Apneas”; 6,586,478 to Ackman, et al., entitled “Methods and Compositions for Improving Sleep”; and 6,525,073 to Mendel, et al., entitled “Prevention or Treatment of Insomnia with a Neurokinin-1 Receptor Antagonist”. Depending upon the particular medication, alternative compounds may be required for use in connection with an implantable drug pump. Routine experimentation may be employed to identify medications for treatment of sleep apnea that are safe and effective for use in connection with an implantable drug pump. Dosages may be titrated based upon the frequency or duration of episodes of apnea.
During the actual episode of apnea/hypopnea, an implantable alarm (such as alarm 18 of
If implantable phrenic nerve stimulators are implanted, apnea/hypopnea therapy can also involve delivery of rhythmic electrical stimulation to the phrenic nerves to mimic breathing (assuming the apnea/hypopnea is due to a lack of phrenic nerve signals.) Examples of phrenic nerve stimulators are set forth in U.S. Pat. No. 5,056,519 to Vince, entitled “Unilateral Diaphragmatic Pacer” and in U.S. Pat. No. 6,415,183 to Scheiner, et al., entitled “Method and Apparatus for Diaphragmatic Pacing”, which are incorporated by reference herein. Other respiratory nerves may be stimulated as well. U.S. Pat. No. 5,911,218 to DiMarco, entitled “Method and Apparatus for Electrical Stimulation of the Respiratory Muscles to Achieve Artificial Ventilation in a Patient” describes stimulation of nerves leading to intercostal muscles.
If an implantable hypoglossyl nerve stimulator is implanted, therapy can also involve delivery of stimulation to the hypoglossyl nerves in response to obstructive sleep apnea. Examples of hypoglossyl nerve stimulators are set forth in U.S. Patent Application 2003/0216789 of Deem et al., entitled “Method and System for Treating Sleep Apnea.”
Insofar as CSR therapy is concerned, CSR often arises due to CHF and so CSR can often be remedied by addressing the underlying CHF. See, e.g. U.S. patent application Ser. No. 10/792,305, filed Mar. 2, 2004, entitled “System And Method For Diagnosing And Tracking Congestive Heart Failure Based On The Periodicity Of Cheyne-Stokes Respiration Using An Implantable Medical Device” (A04P1019). Accordingly, upon detection of episodes CSR, the pacer/ICD preferably employs otherwise conventional techniques to detect CHF and, if CHF is present, any of a variety of therapies directed to mitigating CHF may be implemented by the device. For example, cardiac resynchronization therapy (CRT) may be performed to improve cardiac function. CRT and related therapies are discussed in, for example, U.S. Pat. No. 6,643,546 to Mathis, et al., entitled “Multi-Electrode Apparatus And Method For Treatment Of Congestive Heart Failure”; U.S. Pat. No. 6,628,988 to Kramer, et al., entitled “Apparatus And Method For Reversal Of Myocardial Remodeling With Electrical Stimulation”; and U.S. Pat. No. 6,512,952 to Stahmann, et al., entitled “Method And Apparatus For Maintaining Synchronized Pacing”. CHF therapy may also include delivery of medications via an implantable drug pump, if so equipped. Exemplary CHF medications include ACE inhibitors, diuretics, digitalis and compounds such as captopril, enalapril, lisinopril and quinapril. Depending upon the particular medication, alternative compounds may be required for use in connection with an implantable drug pump. Routine experimentation may be employed to identify medications for treatment of CHF that are safe and effective for use in connection with an implantable drug pump.
Additionally, during an individual episode of CSR, the implantable alarm or external bedside alarm may be triggered to awaken the patient to break the cycle of CSR. Again, activation of an alarm to awaken the patient is preferably employed only if other forms of therapy are found to be ineffective. See, also, U.S. patent application Ser. No. 10/844,023, filed May 11, 2004, entitled “System and Method for Providing Demand-Based Cheyne-Stokes Respiration Therapy Using an Implantable Medical Device” (A04P1042).
Insofar as hyperpnea is concerned, hyperpnea may arise during CSR or may arise during an asthma attack. Hyperpnea arising due to CSR is preferably addressed via CSR therapy. See, also, U.S. patent application Ser. No. 10/829,719, filed Apr. 21, 2004, entitled “System and Method for Applying Therapy during Hyperpnea Phase of Periodic Breathing Using an Implantable Medical Device” (A04P1037). Hyperpnea arising due to asthma may be addressed by addressing the asthma via suitable medications delivered via the implantable drug pump. Examples of asthma medications are set forth, for example, in U.S. Pat. No. 4,089,959 to Diamond, entitled “Long-Acting Xanthine Bronchodilators and Antiallergy Agents”. Depending upon the particular medication, alternative compounds may be required for use in connection with an implantable drug pump. Routine experimentation may be employed to identify medications for treatment of asthma that are safe and effective for use in connection with an implantable drug pump. Dosages may be titrated as needed based on tracking and trending of such breathing patterns.
Additional techniques may be used, if desired, to corroborate the detection of an episode of abnormal respiration made using the techniques of the invention before therapy is delivered. See, e.g., U.S. patent application Ser. No. 10/883,857, filed Jun. 30, 2004, entitled “System And Method For Real-Time Apnea/Hypopnea Detection Using An Implantable Medical System (A04P1057) and U.S. patent application Ser. No. 10/821,241, filed Apr. 7, 2004, entitled “System And Method For Apnea Detection Using Blood Pressure Detected via an Implantable Medical System” (A04P1034).
At step 456, the device also tracks and trends changes in respiration patterns. This may be achieved by continuously monitoring the patient for apneic or hypopneic events and quantifying the amount of apnea based on an index. A commonly used index is the apnea hypopnea index (AHI). This index is based on counting apnea and hypopneas that occur over the entire night and dividing the number of apnea and hypopneas by the total sleep time in hours. This invention provides a surrogate for AHI using the number of IEGM detected apneas and hypopneas divided by the total rest time in hours. The total rest time approximates the total sleep time and is derived measuring the time that a patient is at profound rest by using an activity sensor as set forth in: in aforementioned patent to Bornzin et al. (U.S. Pat. No. 5,476,483.) Alternatively, the total sleep time may be estimated using IEGM based respiratory rate trends. During sleep, the respiration rate diminishes below the wakeful respiration rates and sleep time may be easily determined using the IEGM based breathing rate trend. In fact, by making a histogram of the IEGM breathing rates sampled at equal intervals throughout the day and counting the number of intervals in the lowest mode an estimate of the duration of sleep may be performed. Another method that may be used to estimate the total sleep time throughout the day depends on a direct current (DC) accelerometer to quantify the amount of time that a patient is lying down as set forth in U.S. Pat. No. 6,466,821, to Pianca et al., entitled “AC/DC Multi-Axis Accelerometer for Determining Patient Activity and Body Position”. It is also be possible to use Heart rate dynamics to differentiate between awake and sleep state. See, Redmond et al., “Cardiorespiratory-based sleep staging in subjects with obstructive sleep apnea,” IEEE Trans Biomed Eng 2005; 53(3):485-96.
An exemplary trend pattern is illustrated in
What have been described are various techniques for tracking respiration via IEGM signals, detecting episodes of abnormal respiration and delivering appropriate therapy. For the sake of completeness, a detailed description of an exemplary pacer/ICD for controlling these functions will now be provided. However, principles of invention may be implemented within other pacer/ICD implementations or within other devices. In particular, techniques of the invention are also applicable to detecting respiration via surface EKG signals and hence are not necessarily limited to use with implantable devices. In this regard, it is known that the mean cardiac axis and EKG morphology is influenced by electrode motion relative to the heart and by changes in thoracic electrical impedance as the lungs fill and empty. The sinus rate is modulated by vagal influences in synchronization with respiration. Pressure changes (i.e. breathing-related as well as cardiac cycle-related pressure changes) influence IEGM morphology.
To sense left atrial and ventricular cardiac signals and to provide left chamber pacing therapy, pacer/ICD 10 is coupled to a “coronary sinus” lead 624 designed for placement in the “coronary sinus region” via the coronary sinus os for positioning a distal electrode adjacent to the left ventricle and/or additional electrode(s) adjacent to the left atrium. As used herein, the phrase “coronary sinus region” refers to the vasculature of the left ventricle, including any portion of the coronary sinus, great cardiac vein, left marginal vein, left posterior ventricular vein, middle cardiac vein, and/or small cardiac vein or any other cardiac vein accessible by the coronary sinus. Accordingly, an exemplary coronary sinus lead 624 is designed to receive atrial and ventricular cardiac signals and to deliver left ventricular pacing therapy using at least a left ventricular tip electrode 626, left atrial pacing therapy using at least a left atrial ring electrode 627, and shocking therapy using at least a left atrial coil electrode 628. With this configuration, biventricular pacing can be performed. Although only three leads are shown in
A simplified block diagram of internal components of pacer/ICD 10 is shown in
At the core of pacer/ICD 10 is a programmable microcontroller 660, which controls the various modes of stimulation therapy. As is well known in the art, the microcontroller 660 (also referred to herein as a control unit) typically includes a microprocessor, or equivalent control circuitry, designed specifically for controlling the delivery of stimulation therapy and may further include RAM or ROM memory, logic and timing circuitry, state machine circuitry, and I/O circuitry. Typically, the microcontroller 660 includes the ability to process or monitor input signals (data) as controlled by a program code stored in a designated block of memory. The details of the design and operation of the microcontroller 660 are not critical to the invention. Rather, any suitable microcontroller 660 may be used that carries out the functions described herein. The use of microprocessor-based control circuits for performing timing and data analysis functions are well known in the art.
As shown in
The microcontroller 660 further includes timing control circuitry (not separately shown) used to control the timing of such stimulation pulses (e.g., pacing rate, atrio-ventricular (AV) delay, atrial interconduction (A-A) delay, or ventricular interconduction (V-V) delay, etc.) as well as to keep track of the timing of refractory periods, blanking intervals, noise detection windows, evoked response windows, alert intervals, marker channel timing, etc., which is well known in the art. Switch 674 includes a plurality of switches for connecting the desired electrodes to the appropriate I/O circuits, thereby providing complete electrode programmability. Accordingly, the switch 674, in response to a control signal 680 from the microcontroller 660, determines the polarity of the stimulation pulses (e.g., unipolar, bipolar, combipolar, etc.) by selectively closing the appropriate combination of switches (not shown) as is known in the art.
Atrial sensing circuits 682 and ventricular sensing circuits 684 may also be selectively coupled to the right atrial lead 620, coronary sinus lead 624, and the right ventricular lead 630, through the switch 674 for detecting the presence of cardiac activity in each of the four chambers of the heart. Accordingly, the atrial (ATR. SENSE) and ventricular (VTR. SENSE) sensing circuits, 682 and 684, may include dedicated sense amplifiers, multiplexed amplifiers or shared amplifiers. The switch 674 determines the “sensing polarity” of the cardiac signal by selectively closing the appropriate switches, as is also known in the art. In this way, the clinician may program the sensing polarity independent of the stimulation polarity. Each sensing circuit, 682 and 684, preferably employs one or more low power, precision amplifiers with programmable gain and/or automatic gain control, bandpass filtering, and a threshold detection circuit, as known in the art, to selectively sense the cardiac signal of interest. The automatic gain control enables pacer/ICD 10 to deal effectively with the difficult problem of sensing the low amplitude signal characteristics of atrial or ventricular fibrillation. The outputs of the atrial and ventricular sensing circuits, 682 and 684, are connected to the microcontroller 660 which, in turn, are able to trigger or inhibit the atrial and ventricular pulse generators, 670 and 672, respectively, in a demand fashion in response to the absence or presence of cardiac activity in the appropriate chambers of the heart.
For arrhythmia detection, pacer/ICD 10 utilizes the atrial and ventricular sensing circuits, 682 and 684, to sense cardiac signals to determine whether a rhythm is physiologic or pathologic. As used herein “sensing” is reserved for the noting of an electrical signal, and “detection” is the processing of these sensed signals and noting the presence of an arrhythmia. The timing intervals between sensed events (e.g., P-waves, R-waves, and depolarization signals associated with fibrillation which are sometimes referred to as “F-waves” or “Fib-waves”) are then classified by the microcontroller 660 by comparing them to a predefined rate zone limit (i.e., bradycardia, normal, atrial tachycardia, atrial fibrillation, low rate VT, high rate VT, and fibrillation rate zones) and various other characteristics (e.g., sudden onset, stability, physiologic sensors, and morphology, etc.) in order to determine the type of remedial therapy that is needed (e.g., bradycardia pacing, antitachycardia pacing, cardioversion shocks or defibrillation shocks).
Cardiac signals are also applied to the inputs of an analog-to-digital (A/D) data acquisition system 690. The data acquisition system 690 is configured to acquire intracardiac electrogram signals, convert the raw analog data into a digital signal, and store the digital signals for later processing and/or telemetric transmission to an external device 702. The data acquisition system 690 is coupled to the right atrial lead 620, the coronary sinus lead 624, and the right ventricular lead 630 through the switch 674 to sample cardiac signals across any pair of desired electrodes. The microcontroller 660 is further coupled to a memory 694 by a suitable data/address bus 696, wherein the programmable operating parameters used by the microcontroller 660 are stored and modified, as required, in order to customize the operation of pacer/ICD 10 to suit the needs of a particular patient. Such operating parameters define, for example, pacing pulse amplitude or magnitude, pulse duration, electrode polarity, rate, sensitivity, automatic features, arrhythmia detection criteria, and the amplitude, waveshape and vector of each shocking pulse to be delivered to the patient's heart within each respective tier of therapy. Other pacing parameters include base rate, rest rate and circadian base rate.
Advantageously, the operating parameters of the implantable pacer/ICD 10 may be non-invasively programmed into the memory 694 through a telemetry circuit 700 in telemetric communication with the external device 702, such as a programmer, transtelephonic transceiver or a diagnostic system analyzer. The telemetry circuit 700 is activated by the microcontroller by a control signal 706. The telemetry circuit 700 advantageously allows intracardiac electrograms and status information relating to the operation of pacer/ICD 10 (as contained in the microcontroller 660 or memory 694) to be sent to the external device 702 through an established communication link 704. Pacer/ICD 10 further includes an accelerometer or other physiologic sensor 708, commonly referred to as a “rate-responsive” sensor because it is typically used to adjust pacing stimulation rate according to the exercise state of the patient. However, the physiological sensor 708 may, depending upon its capabilities, further be used to detect changes in cardiac output, changes in the physiological condition of the heart, or diurnal changes in activity (e.g., detecting sleep and wake states) and to detect arousal from sleep. Accordingly, the microcontroller 660 responds by adjusting the various pacing parameters (such as rate, AV Delay, V-V Delay, etc.) at which the atrial and ventricular pulse generators, 670 and 672, generate stimulation pulses. While shown as being included within pacer/ICD 10, it is to be understood that the sensor 708 may also be external to pacer/ICD 10, yet still be implanted within or carried by the patient. A common type of rate responsive sensor is an activity sensor incorporating an accelerometer or a piezoelectric crystal, which is mounted within the housing 640 of pacer/ICD 10. Other types of physiologic sensors are also known, for example, sensors that sense the oxygen content of blood, respiration rate and/or minute ventilation, pH of blood, ventricular gradient, etc.
The pacer/ICD additionally includes a battery 710, which provides operating power to all of the circuits shown in
As further shown in
In the case where pacer/ICD 10 is intended to operate as an implantable cardioverter/defibrillator (ICD) device, it detects the occurrence of an arrhythmia, and automatically applies an appropriate electrical shock therapy to the heart aimed at terminating the detected arrhythmia. To this end, the microcontroller 660 further controls a shocking circuit 716 by way of a control signal 718. The shocking circuit 716 generates shocking pulses of low (up to 0.5 joules), moderate (0.5-10 joules) or high energy (11 to 40 joules), as controlled by the microcontroller 660. Such shocking pulses are applied to the heart of the patient through at least two shocking electrodes, and as shown in this embodiment, selected from the left atrial coil electrode 628, the RV coil electrode 636, and/or the SVC coil electrode 638. The housing 640 may act as an active electrode in combination with the RV electrode 636, or as part of a split electrical vector using the SVC coil electrode 638 or the left atrial coil electrode 628 (i.e., using the RV electrode as a common electrode). Cardioversion shocks are generally considered to be of low to moderate energy level (so as to minimize pain felt by the patient), and/or synchronized with an R-wave and/or pertaining to the treatment of tachycardia. Defibrillation shocks are generally of moderate to high energy level (i.e., corresponding to thresholds in the range of 5-40 joules), delivered asynchronously (since R-waves may be too disorganized), and pertaining exclusively to the treatment of fibrillation. Accordingly, the microcontroller 660 is capable of controlling the synchronous or asynchronous delivery of the shocking pulses.
Microcontroller 60 also includes an IEGM individual feature morphology-based respiration detector 701 for detecting respiration based upon one or more IEGM channel signals using the techniques described above. An abnormal respiration pattern detector 703 is also provided the purposes of detecting apnea, hypopnea, etc. using techniques described above. Additionally, an abnormal respiration therapy controller 705 is provided for controlling therapy in response to an episode of abnormal respiration, again using techniques already described. Depending upon the implementation, the various components may be implemented as separate software modules. However, the modules may be combined so as to permit single modules to perform multiple functions.
Further Abnormal Respiration Detection Techniques
Turning now to
An overview of these abnormal respiration detection techniques is set forth in
Turning now to
It is important to correctly extract morphological and temporal variable from IEGM data to ensure that the variable properly reflects the respiratory modulation. A history of the morphological characteristics can be used to aid in variable extraction.
At step 810, the pacer/ICD examines the temporal and morphological parameters to detect any fused beats and to reject the parameters derived from fused beats, as these parameters may be anomalous. In one example, various sets of histogram bins are stored in memory and used to track the distribution of parameter values. Each memory bin is associated with a range of values. An exemplary set of bins for use with vPDI is illustrated in
At steps 814 and 816 of
At step 818, the pacer/ICD analyzes the corrected temporal and morphological parameters to identify individual respiratory cycles (i.e. breaths) based on cyclical changes therein. As already explained in connection with
Exemplary techniques for detecting respiratory parameters will now be described with respect to
At step 842 of
Turning now to
where □=local mean, and where the local standard deviations are used. In this manner, a moving window normalization is achieved to remove the mean and standard-deviation changes that occur due to body position changes while retaining the relative variations due to respiration.
At block 916, the pacer/CD calculates the power of each variable over a previous epoch of X seconds (e.g. 10 seconds.) This is performed by integrating the variable over the previous epoch of time. These power values are in addition to the respiration power value that is described above with reference to
At black 922, the pacer/ICD compares the various derived parameters and one or more thresholds, as described above with reference to
The techniques of
Also, whereas the techniques of
What have been described are various systems and methods for tracking respiration, detecting episodes of abnormal respiration and delivering therapy in response thereto using an implantable system controlled by a pacer or ICD. However, principles of the invention may be exploiting using other implantable systems or in accordance with other techniques. Thus, while the invention has been described with reference to particular exemplary embodiments, modifications can be made thereto without departing from the scope of the invention.
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|U.S. Classification||600/484, 600/513, 600/481, 600/529, 600/516, 600/483, 600/519, 600/517, 607/25, 600/509, 607/18, 607/20, 607/17|
|International Classification||A61B5/08, A61N1/00, A61B5/04, A61B5/02|
|Cooperative Classification||A61B5/08, A61N1/3601, A61B5/0452, A61B5/411, A61B5/0472, A61N1/365, A61B5/4818, A61B5/0031, A61B5/145, A61B2562/0219, A61B5/0803, A61B5/0816, A61B5/11, A61N1/37, A61B5/02405|
|European Classification||A61B5/024A, A61B5/41B, A61B5/48C8, A61B5/08, A61B5/0452|
|Jun 6, 2006||AS||Assignment|
Owner name: PACESETTER, INC., CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:BHARMI, RUPINDER;BORNZIN, GENE A.;REEL/FRAME:017968/0437
Effective date: 20060526
|Oct 24, 2011||FPAY||Fee payment|
Year of fee payment: 4
|Oct 22, 2015||FPAY||Fee payment|
Year of fee payment: 8